Canonical Allele Identifier: CA2120135699

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113946G= , CM000675.2:g.113113946G=	GRCh38
NC_000013.10:g.113768260G= , CM000675.1:g.113768260G=	GRCh37
NC_000013.9:g.112816261G=	NCBI36
NG_009262.1:g.13156G= , LRG_554:g.13156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.350G= MANE Select	ENSP00000329546.4:p.Arg117=
ENST00000346342.7:c.350G=	ENSP00000329546.3:p.Arg117=
ENST00000375581.3:c.416G=	ENSP00000364731.3:p.Arg139=
ENST00000444337.1:c.*158G=	ENSP00000387669.1:n.*158G=
ENST00000473085.1:n.297G=
ENST00000479674.1:n.683G=
ENST00000541084.5:c.164G=	ENSP00000442051.2:p.Arg55=
NM_000131.4:c.416G= , LRG_554t1:c.416G=	NP_000122.1:p.Arg139=
NM_001267554.1:c.164G=	NP_001254483.1:p.Arg55=
NM_019616.3:c.350G= , LRG_554t2:c.350G=	NP_062562.1:p.Arg117=
NR_051961.1:n.437G=
XM_006719963.2:c.350G=	XP_006720026.1:p.Arg117=
XM_011537474.1:c.350G=	XP_011535776.1:p.Arg117=
XM_011537475.1:c.164G=	XP_011535777.1:p.Arg55=
XM_011537477.1:c.311G=	XP_011535779.1:p.Arg104=
XM_006719963.3:c.395G=	XP_006720026.2:p.Arg132=
XM_011537474.2:c.395G=	XP_011535776.2:p.Arg132=
XM_011537475.2:c.209G=	XP_011535777.2:p.Arg70=
NM_019616.4:c.350G= MANE Select	NP_062562.1:p.Arg117=
NR_051961.2:n.434G=
NM_001267554.2:c.164G=	NP_001254483.1:p.Arg55=